Study Start-up Lead

ICON Clinical Research, LP

Multiple Locations
Study start-up management
Regulatory documentation
Ich-gcp compliance
The Study Start-up/Site Activation Lead is responsible at country level for managing and conducting start-up activities in compliance with the client procedures, documents, local and international guidelines such as ICH – GCP and relevant regulations

Job Summary

  • The Study Start-up/Site Activation Lead is responsible at country level for managing and conducting start-up activities in compliance with the client procedures, documents, local and international guidelines such as ICH – GCP and relevant regulations.
  • Accountable for study start-up and regulatory maintenance being in charge with collection, preparation, review and tracking of documents for the application process.
  • In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

The Study Start-up/Site Activation Lead is responsible at country level for managing and conducting start-up activities in compliance with the client procedures, documents, local and international guidelines such as ICH – GCP and relevant regulations.

Skills & Requirements

Must-have

  • Study start-up management
  • Regulatory documentation
  • ICH-GCP compliance
  • Site activation
  • Clinical trial management system (CTMS)

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Team collaboration
  • Work-life balance focus

Key Requirements

  • Bachelor's Degree in life sciences
  • Minimum 5 years clinical research experience
  • Focus on Start-Up
  • Strong project management skills
  • Excellent communication abilities
  • Ability to work to tight deadlines

Work Rights

Not specified

Tailored Resume

Cover Letter